RU2412191C2 - Продукты окислительной деструкции кальций аторвастатина - Google Patents
Продукты окислительной деструкции кальций аторвастатина Download PDFInfo
- Publication number
- RU2412191C2 RU2412191C2 RU2007105689A RU2007105689A RU2412191C2 RU 2412191 C2 RU2412191 C2 RU 2412191C2 RU 2007105689 A RU2007105689 A RU 2007105689A RU 2007105689 A RU2007105689 A RU 2007105689A RU 2412191 C2 RU2412191 C2 RU 2412191C2
- Authority
- RU
- Russia
- Prior art keywords
- atorvastatin
- fluorophenyl
- phenyl
- isopropyl
- atv
- Prior art date
Links
- 0 CC(C)C(C1(C(Nc2ccccc2)=O)OC11c2ccccc2)(O)OC1(c1ccc(*)cc1)O Chemical compound CC(C)C(C1(C(Nc2ccccc2)=O)OC11c2ccccc2)(O)OC1(c1ccc(*)cc1)O 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/14—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/36—Oxygen or sulfur atoms
- C07D207/40—2,5-Pyrrolidine-diones
- C07D207/416—2,5-Pyrrolidine-diones with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to other ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D301/00—Preparation of oxiranes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/48—Compounds containing oxirane rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Epoxy Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SIP200400209 | 2004-07-16 | ||
SI200400209 | 2004-07-16 | ||
SIP200400348 | 2004-12-24 | ||
SI200400348 | 2004-12-24 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2007105689A RU2007105689A (ru) | 2008-08-27 |
RU2412191C2 true RU2412191C2 (ru) | 2011-02-20 |
Family
ID=35457712
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2007105689A RU2412191C2 (ru) | 2004-07-16 | 2005-07-15 | Продукты окислительной деструкции кальций аторвастатина |
Country Status (14)
Country | Link |
---|---|
US (4) | US8044086B2 (ja) |
EP (1) | EP1771455B1 (ja) |
JP (1) | JP5000502B2 (ja) |
CN (1) | CN1997651B (ja) |
AU (1) | AU2005263550C1 (ja) |
BR (1) | BRPI0513396A (ja) |
CA (2) | CA2573969C (ja) |
ES (1) | ES2586561T3 (ja) |
HU (1) | HUE029911T2 (ja) |
MX (1) | MX2007000582A (ja) |
PL (1) | PL1771455T3 (ja) |
RU (1) | RU2412191C2 (ja) |
SI (1) | SI1771455T1 (ja) |
WO (1) | WO2006008091A2 (ja) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW200825092A (en) * | 2004-09-28 | 2008-06-16 | Teva Pharma | A method for reducing the level of AED in atorvastatin calcium sample |
DE602006014193D1 (de) | 2005-11-21 | 2010-06-17 | Warner Lambert Co | Neue formen von är-(r*,r*)ü-2-(4-fluorphenyl)-b,d-dihydroxy-5-(1-methylethyl)-3-phenyl-4-ä(phenylamino)carbonylü-1h-pyrrol-1-heptansäure-magnesium |
US20070265456A1 (en) * | 2006-05-09 | 2007-11-15 | Judith Aronhime | Novel crystal forms of atorvastatin hemi-calcium and processes for their preparation as well as novel processes for preparing other forms |
IS8607A (is) * | 2007-02-09 | 2008-08-10 | Actavis Group Hf. | Stöðugar atorvastatin samsetningar |
WO2011077843A1 (ja) * | 2009-12-25 | 2011-06-30 | 沢井製薬株式会社 | アトルバスタチン含有被覆製剤 |
CN110646550B (zh) * | 2018-06-26 | 2022-12-02 | 北京伟林恒昌医药科技有限公司 | 一种阿托伐他汀钙中有关物质的检测方法 |
CN115754025B (zh) * | 2021-09-02 | 2024-07-02 | 上虞京新药业有限公司 | 一种匹伐他汀钙中基因毒性杂质gti的检测方法 |
Family Cites Families (47)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3114497A (en) * | 1962-05-18 | 1963-12-17 | Kugler Emanuel | Drawstring bag |
US5003080A (en) * | 1988-02-22 | 1991-03-26 | Warner-Lambert Company | Process for trans-6-(2-(substituted-pyrrol-1-yl)alkyl)pryan-2-one inhibitors of cholesterol synthesis |
US5216174A (en) * | 1988-02-22 | 1993-06-01 | Warner-Lambert Co. | Process for trans-6-[12-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis |
US5245047A (en) * | 1988-02-22 | 1993-09-14 | Warner-Lambert Company | Process for trans-6-[2-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis |
US5124482A (en) * | 1988-02-22 | 1992-06-23 | Warner-Lambert Company | Process for trans-6-(2-substituted-pyrrol-1-yl)alkyl)pyran-2-one inhibitors of cholesterol synthesis |
US5097045A (en) * | 1989-02-01 | 1992-03-17 | Warner-Lambert Company | Process for trans-6-[2-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis |
US5149837A (en) * | 1988-02-22 | 1992-09-22 | Warner-Lambert Company | Process for trans-6-[2-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis |
FI94339C (fi) * | 1989-07-21 | 1995-08-25 | Warner Lambert Co | Menetelmä farmaseuttisesti käyttökelpoisen /R-(R*,R*)/-2-(4-fluorifenyyli)- , -dihydroksi-5-(1-metyylietyyli)-3-fenyyli-4-/(fenyyliamino)karbonyyli/-1H-pyrroli-1-heptaanihapon ja sen farmaseuttisesti hyväksyttävien suolojen valmistamiseksi |
US5248793A (en) * | 1990-10-17 | 1993-09-28 | Warner-Lambert Company | Process for the synthesis of (4R-cis)-1,1-dimethylethyl 6-iodomethyl or 6-(phenyl-substituted)sulfonyloxymethyl-2,2-dimethyl-1,3-dioxane-4-acetate |
US5103024A (en) * | 1990-10-17 | 1992-04-07 | Warner-Lambert Company | Process for the synthesis of (4r-cis)-1,1-dimethylethyl 6-cyanomethyl-2,2-dimethyl-1,3-dioxane-4-acetate |
US5155251A (en) * | 1991-10-11 | 1992-10-13 | Warner-Lambert Company | Process for the synthesis of (5R)-1,1-dimethylethyl-6-cyano-5-hydroxy-3-oxo-hexanoate |
DK0680320T3 (da) * | 1993-01-19 | 1999-10-25 | Warner Lambert Co | Stabilt oralt CI-981-præparat og fremgangsmåde til fremstilling deraf |
US5298627A (en) * | 1993-03-03 | 1994-03-29 | Warner-Lambert Company | Process for trans-6-[2-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis |
HRP960313B1 (en) * | 1995-07-17 | 2002-08-31 | Warner Lambert Co | Form iii crystalline (r- (r*, r*)-2- (4-fluorophenyl) -beta-delta-hydroxy-5-(1-methylethyl) -3-phenyl-4- ((phenylamino) carbonyl -1h-pyrrole-1-heptanoic acid calcium salt (2:1) |
HRP960312B1 (en) * | 1995-07-17 | 2001-10-31 | Warner Lambert Co | NOVEL PROCESS FOR THE PRODUCTION OF AMORPHOUS /R-(R*, R*)/-2-(4-FLUOROPHENYL)-"beta", "delta"-DIHYDROXY-5-PHENYL-4-/(PHENYLAMINO)CARBONYL/-1H-PYRROLE -1-HEPTANOIC ACID CALCIUM SALT (2 : 1) |
WO1997003959A1 (en) * | 1995-07-17 | 1997-02-06 | Warner-Lambert Company | Crystalline [r-(r*,r*)]-2-(4-fluorophenyl)-beta,delta-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1h-pyrrole-1-heptanoic acid hemi calcium salt (atorvastatin) |
AU755543B2 (en) * | 1997-12-19 | 2002-12-12 | Warner-Lambert Export Limited | Process for the synthesis of 1,3-diols |
IN191236B (ja) * | 1999-05-25 | 2003-10-11 | Ranbaxy Lab Ltd | |
US6646133B1 (en) * | 2000-10-17 | 2003-11-11 | Egis Gyogyszergyar Rt. | Process for the preparation of amorphous atorvastatin calcium |
NZ518822A (en) | 1999-11-04 | 2004-12-24 | Andrx Corp | Treating a mammal with an APP processing disorder such as Alzheimer's Disease and Down's Syndrome by administering at least one HMG-CoA reductase inhibitor |
WO2001037876A2 (en) | 1999-11-24 | 2001-05-31 | Bayer Aktiengesellschaft | Methods of ameliorating abnormal bone states |
SI20425A (sl) * | 1999-12-10 | 2001-06-30 | LEK tovarna farmacevtskih in kemi�nih izdelkov d.d. | Priprava amorfnega atorvastatina |
DE60026737T2 (de) * | 1999-12-17 | 2006-09-21 | Pfizer Science And Technology Ireland Ltd., Dun Laoghaire | Verfahren zur herstellung von kristallin atorvastin kalcium |
MXPA02004078A (es) * | 1999-12-17 | 2002-10-11 | Warner Lambert Res & Dev | Un proceso a escala industrial para producir sal de hemi calcio de trihidrato de atorvastatin cristalino. |
WO2001045674A1 (en) * | 1999-12-20 | 2001-06-28 | Cocensys, Inc. | Process for producing nanometer particles by fluid bed spray-drying |
WO2001058443A1 (en) | 2000-02-10 | 2001-08-16 | Takeda Chemical Industries, Ltd. | TNF- α INHIBITORS |
CA2426632C (en) * | 2000-11-03 | 2008-08-05 | Teva Pharmaceutical Industries, Ltd. | Atorvastatin hemi-calcium form vii |
ES2313999T3 (es) * | 2000-11-16 | 2009-03-16 | Teva Pharmaceutical Industries Ltd. | Hidrolisis de esteres del acido (r(r*,r*))-2-(4-fluorofenil)-beta, delta-dihidroxi-5-(1-metiletil)-3-fenil-4-((fenilamino)carbonil)-1h-pirrol-1-heptanoico con hidroxido calcico. |
US7501450B2 (en) * | 2000-11-30 | 2009-03-10 | Teva Pharaceutical Industries Ltd. | Crystal forms of atorvastatin hemi-calcium and processes for their preparation as well as novel processes for preparing other forms |
IL156055A0 (en) * | 2000-11-30 | 2003-12-23 | Teva Pharma | Novel crystal forms of atorvastatin hemi calcium and processes for their preparation as well as novel processes for preparing other forms |
ATE420070T1 (de) * | 2000-12-27 | 2009-01-15 | Teva Pharma | Kristalline formen von atorvastatin |
US6476235B2 (en) * | 2001-01-09 | 2002-11-05 | Warner-Lambert Company | Process for the synthesis of 5-(4-fluorophenyl)-1-[2-((2R,4R)-4-hydroxy-6-oxo-tetrahydro-pyran-2-yl)-ethyl]-2-isopropyl-4-phenyl-1H-pyrrole-3-carboxylic acid phenylamide |
WO2002057229A1 (en) * | 2001-01-19 | 2002-07-25 | Biocon India Limited | FORM V CRYSTALLINE [R-(R*,R*)]-2-(4-FLUOROPHENYL)-ß,$G(D)-DIHYDROXY-5-(1-METHYLETHYL)-3-PHENYL-4-[(PHENYLAMINO)CARBONYL]-1H-PYRROLE-1- HEPTANOIC ACID HEMI CALCIUM SALT. (ATORVASTATIN) |
SI20814A (sl) * | 2001-01-23 | 2002-08-31 | LEK, tovarna farmacevtskih in kemi�nih izdelkov, d.d. | Priprava amorfnega atorvastatina |
CZ2004126A3 (cs) * | 2001-07-30 | 2004-12-15 | Dr. Reddy's Laboratories Limited | Krystalické formy VI. A VII. vápenaté soli atorvastatinu |
US7074818B2 (en) * | 2001-07-30 | 2006-07-11 | Dr. Reddy's Laboratories Limited | Crystalline forms VI and VII of Atorvastatin calcium |
PE20030324A1 (es) * | 2001-07-31 | 2003-04-03 | Warner Lambert Co | Composiciones farmaceuticas de amlodipina y atorvastatina |
CA2456095C (en) * | 2001-08-31 | 2010-05-11 | Morepen Laboratories Ltd. | An improved process for the preparation of amorphous atorvastatin calcium salt (2:1) |
UA77990C2 (en) * | 2001-12-12 | 2007-02-15 | Crystalline calcium salt of (2:1) [r-(r*,r*)]-2-(4-fluorophenyl)-?,?-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1h-pyrroleheptanic acid | |
CZ296967B6 (cs) * | 2002-02-01 | 2006-08-16 | Zentiva, A.S. | Zpusob výroby amorfní formy hemivápenaté soli (3R,5R) 7-[3-fenyl-4-fenylkarbamoyl-2-(4-fluorfenyl)-5-isopropylpyrrol-1-yl]-3,5-dihydroxyheptanové kyseliny (atorvastatinu) |
IL163594A0 (en) * | 2002-02-19 | 2005-12-18 | Teva Pharma | Processes for desolvating solvates of atorvastatinhemi-calcium and atorvastatin hemi-calcium essentially free of organic solvent |
ITMI20020907A1 (it) * | 2002-04-29 | 2003-10-29 | Chemi Spa | Processo di preparazione della forma amorfa del sale di calcio della atorvastatina |
EP1562583A1 (en) * | 2002-09-03 | 2005-08-17 | Morepen Laboratories Ltd. | Atorvastatin calcium form vi or hydrates thereof |
SI21302A (sl) | 2002-10-11 | 2004-04-30 | LEK farmacevtska dru�ba d.d. | Stabiliziran farmacevtski izdelek z amorfno aktivno učinkovino |
AU2003297594A1 (en) * | 2002-11-28 | 2004-06-23 | Teva Pharmaceutical Industries Ltd. | Crystalline form f of atorvastatin hemi-calcium salt |
HU227041B1 (en) * | 2003-03-24 | 2010-05-28 | Richter Gedeon Nyrt | Process for the synthesis of amorphous atorvastatin calcium |
CA2627940A1 (en) * | 2004-03-17 | 2005-10-06 | Ranbaxy Laboratories Limited | Process for the production of atorvastatin calcium in amorphous form |
-
2005
- 2005-07-15 JP JP2007520774A patent/JP5000502B2/ja not_active Expired - Fee Related
- 2005-07-15 HU HUE05760907A patent/HUE029911T2/en unknown
- 2005-07-15 CA CA2573969A patent/CA2573969C/en not_active Expired - Fee Related
- 2005-07-15 CN CN2005800240856A patent/CN1997651B/zh not_active Expired - Fee Related
- 2005-07-15 US US11/632,608 patent/US8044086B2/en not_active Expired - Fee Related
- 2005-07-15 WO PCT/EP2005/007739 patent/WO2006008091A2/en active Application Filing
- 2005-07-15 CA CA 2833770 patent/CA2833770A1/en not_active Abandoned
- 2005-07-15 SI SI200532085A patent/SI1771455T1/sl unknown
- 2005-07-15 AU AU2005263550A patent/AU2005263550C1/en not_active Ceased
- 2005-07-15 EP EP05760907.5A patent/EP1771455B1/en not_active Revoked
- 2005-07-15 ES ES05760907.5T patent/ES2586561T3/es active Active
- 2005-07-15 PL PL05760907.5T patent/PL1771455T3/pl unknown
- 2005-07-15 RU RU2007105689A patent/RU2412191C2/ru active
- 2005-07-15 MX MX2007000582A patent/MX2007000582A/es active IP Right Grant
- 2005-07-15 BR BRPI0513396-3A patent/BRPI0513396A/pt not_active Application Discontinuation
-
2009
- 2009-11-06 US US12/613,787 patent/US20100056605A1/en not_active Abandoned
-
2010
- 2010-04-30 US US12/771,726 patent/US20100219063A1/en not_active Abandoned
-
2014
- 2014-12-18 US US14/575,339 patent/US9453030B2/en active Active
Non-Patent Citations (1)
Title |
---|
HURLEY Т R et al: "Photodecomposition of CI-981, an HMG-CoA reductase inhibitor", TETRAHEDRON, ELSEVIER SCIENCE PUBLISHERS, AMSTERDAM, NL, vol.49, no.10, 05.03.1993. Organische Chemie 1990, SS.648-651. * |
Also Published As
Publication number | Publication date |
---|---|
HUE029911T2 (en) | 2017-04-28 |
JP2008506655A (ja) | 2008-03-06 |
SI1771455T1 (sl) | 2016-09-30 |
CA2573969C (en) | 2014-02-04 |
CN1997651A (zh) | 2007-07-11 |
AU2005263550B2 (en) | 2011-11-03 |
CA2833770A1 (en) | 2006-01-26 |
WO2006008091A3 (en) | 2006-09-08 |
ES2586561T3 (es) | 2016-10-17 |
MX2007000582A (es) | 2007-03-30 |
AU2005263550C1 (en) | 2013-01-17 |
EP1771455A2 (en) | 2007-04-11 |
US9453030B2 (en) | 2016-09-27 |
WO2006008091A2 (en) | 2006-01-26 |
US20100056605A1 (en) | 2010-03-04 |
PL1771455T3 (pl) | 2016-11-30 |
AU2005263550A1 (en) | 2006-01-26 |
CA2573969A1 (en) | 2006-01-26 |
US8044086B2 (en) | 2011-10-25 |
CN1997651B (zh) | 2012-06-06 |
BRPI0513396A (pt) | 2008-05-06 |
EP1771455B1 (en) | 2016-05-11 |
US20070208071A1 (en) | 2007-09-06 |
US20100219063A1 (en) | 2010-09-02 |
RU2007105689A (ru) | 2008-08-27 |
US20150105551A1 (en) | 2015-04-16 |
JP5000502B2 (ja) | 2012-08-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US9453030B2 (en) | Oxidative degradation products of atrovastatin calcium | |
CN111094299B (zh) | 雷帕霉素衍生物 | |
EP1634877B1 (en) | Mixture and compounds from mycelia of antrodia camphorata and use thereof | |
KR100881103B1 (ko) | 실질적으로 불순물을 함유하지 않는 아토르바스타틴 칼슘의형태를 제조하는 방법 | |
RU2752568C2 (ru) | Новые антимикробные соединения, их применение для лечения инфекций млекопитающих и новый метаболический механизм | |
WO2017017048A1 (en) | Analogs of adamantylureas as soluble epoxide hydrolase inhibitors | |
US20110112165A1 (en) | Atorvastatin-aliskiren | |
EA013500B1 (ru) | Способ получения аморфной кальциевой соли аторвастатина | |
Belwal et al. | Isolation, identification, and characterization of an unknown impurity in lovastatin EP | |
EP1667974B1 (en) | Process for producing high purity 3,5-dihydroxy-6-heptenoic acid derivative | |
Dhivare et al. | Synthesis of new series of N-substituted phenyl succinimide and glutarimide derivatives for the study of their antifungal activity | |
US20160039871A1 (en) | Novel forms of telaprevir | |
US20210221777A1 (en) | Novel compounds related to mycothiazole and methods of treating cancer | |
EA021034B1 (ru) | Применение аторвастатин лактолов в лечении состояний, которые модулируются 3-гидрокси-3-метилглютарил-коэнзим а редуктазой | |
FR2510569A1 (fr) | Compose cytostatique et procede de preparation |